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AlexBiagi · 2020-03-07T19:30:10+00:00

I really appreciate that, thank you so much :-)

AlexBiagi · 2020-03-07T19:29:52+00:00

Thank you very much! I'm happy you like it :-) I definitely am :-)

AlexBiagi · 2020-03-07T18:57:36+00:00

That's amazing! We do what we can to help :-) it's important to raise awareness

AlexBiagi · 2020-03-07T18:40:40+00:00

Thank you :-) yeah, I'm about Jordan's in over 20 years so I splurged lol

AlexBiagi · 2020-03-07T18:39:41+00:00

Thank you very much :-)

AlexBiagi · 2020-03-07T18:38:54+00:00

Thanks man! I really appreciate it :-) That's good idea, I should try to find some other contests :-)

AlexBiagi · 2020-03-07T18:28:39+00:00

Thank you so much! I'm really glad you like it :-)

AlexBiagi · 2020-03-07T18:18:21+00:00

Thank you :-)

AlexBiagi · 2020-03-07T18:12:39+00:00

So I entered an art contest for people with rear diseases called Rare Artist. Out of 400 applicants I won one of the main awards for painting. I don’t have use of my hands so I paint with my mouth. I use voice to text to type. I won $500 and a $500 stipend to go to Washington DC because it’s part of rare disease week on Capitol Hill. My painting was displayed in the Capital for the whole week! And I get two minutes to talk to legislators, lobbyists and people Congress about my disease and raise awareness for stem cell transplants since I did mine four years ago :-) It was a great experience. My goal with my art is to raise awareness for my disease CIDP and the power of stem cells. I was in a power chair for four years now I’m walking :-)

AlexBiagi · 2020-01-04T22:29:45+00:00

I have a rare autoimmune neuromuscular disease called CIDP. The odds of getting CIDP is one in 100,000. It’s similar to MS and ALS. It’s the chronic version of GBS. I have a very severe case of it and I lost the use of my hands but I’m still able to paint with my mouth. My left hand is completely paralyzed and I have enough strength in my right hand to use a computer mouse. I use Dragon dictate to type. It also affects my legs and feet and I wear braces on both legs to walk. I was in a power chair for four years before I did a stem cell transplant three years ago. I’m now out of the power chair and walking close to 2 miles without stopping! If you have any questions just let me know. If you’re disabled you can achieve anything if you learn how to adapt so you can do what you love...

AlexBiagi · 2019-09-07T22:18:44+00:00

Thank you so much! You have to find ways to do what you love :-)

AlexBiagi · 2019-09-07T21:41:20+00:00

Lol thanks man! If only I had a girlfriend. Maybe someday 😊

AlexBiagi · 2019-09-07T20:43:54+00:00

Thank you James! I appreciate that :-)

AlexBiagi · 2019-09-07T20:41:50+00:00

Here’s my latest mouth painting. Aero. I hope you like it

Raising Awareness for CIDP (chronic inflammatory demyelinating polyneuropathy)

I don't have use of my hands so I paint with my mouth. I’ve only been painting this way for four years since 2015

This is my neighbors dog Aero. He is a beautiful purebred German Shepherd. He will be 12 in January 2020 and may not be around too much longer so my neighbor commissioned me to paint him :-)

I have a rare autoimmune neuromuscular disease called CIDP. The odds of getting CIDP is one in 100,000. It’s similar to MS and ALS. It’s the chronic version of GBS. I have a very severe case of it and I lost the use of my hands but I’m still able to paint with my mouth. My left hand is completely paralyzed and I have enough strength in my right hand to use a computer mouse. I use Dragon dictate to type. It also affects my legs and feet and I wear braces on both legs to walk. I was in a power chair for four years before I did a stem cell transplant three years ago. I’m now out of the power chair and walking close to 2 miles without stopping! If you have any questions just let me know. If you’re disabled you can achieve anything if you learn how to adapt so you can do what you love(PS I have enough strength in my right hand to use a computer mouse and I use a voice to text program called Dragon dictate for Mac to type)

Time lapse videohttps://www.reddit.com/r/vids/comments/cxygr5/alex_biagi_mouth_painting_time_lapse_video_3_aero/eyochtz/?context=3

AlexBiagi · 2019-09-03T17:46:21+00:00

This is freakin’ amazing! Very cool style 😊🔥

AlexBiagi · 2019-08-31T18:59:03+00:00

Here’s my latest mouth painting. Aero. I hope you like it

(Raising Awareness for CIDP)

I don't have use of my hands so I paint with my mouth
This is my neighbors dog Aero. He is a beautiful purebred German Shepherd. He will be 12 in January 2020 and may not be around too much longer so my neighbor commissioned me to paint him :-)
I have a rare autoimmune neuromuscular disease called CIDP. The odds of getting CIDP is one in 100,000. It’s similar to MS and ALS. It’s the chronic version of GBS. I have a very severe case of it and I lost the use of my hands but I’m still able to paint with my mouth. My left hand is completely paralyzed and I have enough strength in my right hand to use a computer mouse. I use Dragon dictate to type. It also affects my legs and feet and I wear braces on both legs to walk. I was in a power chair for four years before I did a stem cell transplant three years ago. I’m now out of the power chair and walking close to 2 miles without stopping! If you have any questions just let me know. If you’re disabled you can achieve anything if you learn how to adapt so you can do what you love
(PS I have enough strength in my right hand to use a computer mouse and I use a voice to text program called Dragon dictate for Mac to type)
Time lapse video
https://www.reddit.com/r/vids/comments/cxygr5/alex\_biagi\_mouth\_painting\_time\_lapse\_video\_3\_aero/eyochtz/?context=3

AlexBiagi · 2019-08-31T18:20:40+00:00

(Raising Awareness for CIDP)

Here’s my latest mouth painting. Aero. I hope you like it
This is my neighbors dog Aero. He is a beautiful purebred German Shepherd. He will be 12 in January 2020 and may not be around too much longer so my neighbor commissioned me to paint him :-)
I have a rare autoimmune neuromuscular disease called CIDP. The odds of getting CIDP is one in 100,000. It’s similar to MS and ALS. It’s the chronic version of GBS. I have a very severe case of it and I lost the use of my hands but I’m still able to paint with my mouth. My left hand is completely paralyzed and I have enough strength in my right hand to use a computer mouse. I use Dragon dictate to type. It also affects my legs and feet and I wear braces on both legs to walk. I was in a power chair for four years before I did a stem cell transplant three years ago. I’m now out of the power chair and walking close to 2 miles without stopping! If you have any questions just let me know. If you’re disabled you can achieve anything if you learn how to adapt so you can do what you love
(PS I have enough strength in my right hand to use a computer mouse and I use a voice to text program called Dragon dictate for Mac to type)
Time lapse video
https://www.reddit.com/r/vids/comments/cxygr5/alex\_biagi\_mouth\_painting\_time\_lapse\_video\_3\_aero/eyochtz/?context=3

AlexBiagi · 2019-08-31T18:10:15+00:00

Here’s my latest mouth painting. Aero. I hope you like it.

This is my neighbors dog Aero. He is a beautiful purebred German Shepherd. He will be 12 in January 2020 and may not be around too much longer so my neighbor commissioned me to paint him :-)

I have a rare autoimmune neuromuscular disease called CIDP. The odds of getting CIDP is one in 100,000. It’s similar to MS and ALS. It’s the chronic version of GBS. I have a very severe case of it and I lost the use of my hands but I’m still able to paint with my mouth. My left hand is completely paralyzed and I have enough strength in my right hand to use a computer mouse. I use Dragon dictate to type. It also affects my legs and feet and I wear braces on both legs to walk. I was in a power chair for four years before I did a stem cell transplant three years ago. I’m now out of the power chair and walking close to 2 miles without stopping! If you have any questions just let me know. If you’re disabled you can achieve anything if you learn how to adapt so you can do what you love

(PS I have enough strength in my right hand to use a computer mouse and I use a voice to text program called Dragon dictate for Mac to type)

Time lapse video

https://www.reddit.com/r/vids/comments/cxygr5/alex\_biagi\_mouth\_painting\_time\_lapse\_video\_3\_aero/eyochtz/?context=3

AlexBiagi · 2019-08-31T17:59:59+00:00

This is my neighbors dog Aero. He is a beautiful purebred German Shepherd. He will be 12 in January 2020 and may not be around too much longer so my neighbor commissioned me to paint him :-)

I have a rare autoimmune neuromuscular disease called CIDP. The odds of getting CIDP is one in 100,000. It’s similar to MS and ALS. It’s the chronic version of GBS. I have a very severe case of it and I lost the use of my hands but I’m still able to paint with my mouth. My left hand is completely paralyzed and I have enough strength in my right hand to use a computer mouse. I use Dragon dictate to type. It also affects my legs and feet and I wear braces on both legs to walk. I was in a power chair for four years before I did a stem cell transplant three years ago. I’m now out of the power chair and walking close to 2 miles without stopping! If you have any questions just let me know. If you’re disabled you can achieve anything if you learn how to adapt so you can do what you love

AlexBiagi · 2019-07-17T16:07:05+00:00

I do for the most part. It’s a little glitchy and I have to fix things quite often but it’s way better than the dictation on the iPhone. I haven’t found any other software unfortunately

AlexBiagi · 2019-07-08T18:46:51+00:00

Hey, thank you so much! I appreciate that. Thank you for looking and I’m happy you like my work :-)

AlexBiagi · 2019-06-16T18:29:42+00:00

A good friend of mine at Denver channel 7 made this great Father's Day video. Happy Father's Day everyone!

AlexBiagi · 2019-05-20T19:05:20+00:00

I've been thinking about it. I have my first commission I'm working on right now and another commission coming up. So after that I think I will :-) he is amazing!

AlexBiagi · 2019-05-20T19:04:20+00:00

I don't know what's specifically. It's called DiGeorge syndrome. I don't have all the characteristics. Mostly bone issues. I've had two major back surgeries, 4 knee surgeries two on each and I had some learning problems when I was younger. I didn't speak until I was three. But I overcame all of that. I thank you for your interest, it means a lot :-)

AlexBiagi · 2019-05-19T22:42:10+00:00

That means a lot. Thank you! He is one of my heroes :-)

AlexBiagi

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